Screening and Identification of Biomarkers for High Myopia by a Rapid Method
Study Details
Study Description
Brief Summary
To screen and identify sensitive biomarkers for high myopia via a robust, convenient, and cost-effective approach according to the association between high myopia and concentration of biomarkers in tear fluid, saliva and blood among adults and children.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Detailed Description
Myopia has emerged as a serious public health issue, with the prevalence increasing rapidly worldwide, especially in East Asia. Increasingly early onset of myopia leads to high myopia with sight-threatening complications (e.g., secondary cataracts, glaucoma, and retinal detachment) that cannot be treated by optical means.
A key goal of myopia research over the past decades has been to identify those sensitive biomarkers. Accurate monitoring of myopic-specific biomarkers is desirable for achieving early diagnosis, progression assessment, and prognostic management.
However, measurement of levels of MMPs in human have been restricted to aqueous humors, which is invasive and the findings are difficult to be replicated in other studies. In order to achieve the goal of convenient high myopic detection, the use of a panel of biomarkers using a multiplex approach may indeed be rapid and highly reproducible with potentially higher sensitivity and specificity than single biomarkers, such as MMP 2 for the early detection of high myopia.
In this study we have used a newly developed immunoassay technology, and identified a panel of novel biomarkers for early detection of high myopia by non-invasively evaluating several biomarkers that are measurable in the saliva and tear fluid of adults.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Emmetropic subjects Spherical equivalent (Diopter, D) to be between -0.5 and +0.5 D |
Diagnostic Test: blood sample
Blood collection Circulating serum concentrations of melatonin and dopamine were determined from fasting blood samples. Participants were required to fast from 10 pm the previous evening. A 5 mL serum blood sample was collected from the antecubital vein between 8.30 am and 10 am.
Tear collection Tear samples were collected using Schirmer's strip without anesthesia between 8:30-10:00am. Tears were extracted in 200 μl of 1 X Phosphate Buffered Saline with 0.1% Tween-20 (PBST).
Saliva collection Saliva samples were collected via the "passive drool" method with subjects in a seated position. Subjects were asked to rinse their mouth with water 10 minutes prior to saliva collection and to refrain from using lip makeup during the sampling period.
Other Names:
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| Low and moderate myopic subjects Spherical equivalent (Diopter, D) to be less than -0.5 but over -6.0D |
Diagnostic Test: blood sample
Blood collection Circulating serum concentrations of melatonin and dopamine were determined from fasting blood samples. Participants were required to fast from 10 pm the previous evening. A 5 mL serum blood sample was collected from the antecubital vein between 8.30 am and 10 am.
Tear collection Tear samples were collected using Schirmer's strip without anesthesia between 8:30-10:00am. Tears were extracted in 200 μl of 1 X Phosphate Buffered Saline with 0.1% Tween-20 (PBST).
Saliva collection Saliva samples were collected via the "passive drool" method with subjects in a seated position. Subjects were asked to rinse their mouth with water 10 minutes prior to saliva collection and to refrain from using lip makeup during the sampling period.
Other Names:
|
| High myopic subjects Spherical equivalent (Diopter, D) to be over or equal to -6.0D |
Diagnostic Test: blood sample
Blood collection Circulating serum concentrations of melatonin and dopamine were determined from fasting blood samples. Participants were required to fast from 10 pm the previous evening. A 5 mL serum blood sample was collected from the antecubital vein between 8.30 am and 10 am.
Tear collection Tear samples were collected using Schirmer's strip without anesthesia between 8:30-10:00am. Tears were extracted in 200 μl of 1 X Phosphate Buffered Saline with 0.1% Tween-20 (PBST).
Saliva collection Saliva samples were collected via the "passive drool" method with subjects in a seated position. Subjects were asked to rinse their mouth with water 10 minutes prior to saliva collection and to refrain from using lip makeup during the sampling period.
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Concentration of TNF-α in tear fluid, saliva and blood sample among emmetropic, low and moderate myopic, and high myopic groups [June 30, 2023]
TNF-α: Tumor necrosis factor is an adipokine and a cytokine.
Secondary Outcome Measures
- Concentration of IL-1 in tear fluid, saliva and blood sample among emmetropic, low and moderate myopic, and high myopic groups [June 30, 2023]
IL-1: Interleukin 1
Other Outcome Measures
- Concentration of IL-10 in tear fluid, saliva and blood sample among emmetropic, low and moderate myopic, and high myopic groups [June 30, 2023]
IL-10: Interleukin 10, an anti-inflammatory cytokine
- Concentration of IL-6 in tear fluid, saliva and blood sample among emmetropic, low and moderate myopic, and high myopic groups [June 30, 2023]
IL-6: Interleukin 6, a pro-inflammatory cytokine
- Concentration of TIMP in tear fluid, saliva and blood sample among emmetropic, low and moderate myopic, and high myopic groups [June 30, 2023]
TIMP: Tissue inhibitor of metalloproteinases, a family of proteins that act as enzyme inhibitors
- Concentration of MMP2 in tear fluid, saliva and blood sample among emmetropic, low and moderate myopic, and high myopic groups [June 30, 2023]
MMP2: Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes
- Concentration of EGF in tear fluid, saliva and blood sample among emmetropic, low and moderate myopic, and high myopic groups [June 30, 2023]
EGF:Epidermal growth factor (EGF) is a protein that stimulates cell growth.
Eligibility Criteria
Criteria
Children Inclusion Criteria
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Children aged 6-17
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Removing flexible lenses for at least 1 week, flexible astigmatism and hard lenses for at least 3 weeks, orthokeratology lenses for at least 3 months;
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Best corrected visual acuity of either eye were all ≥ 1.0;
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The range of myopia in either eye was -15 D ≤ SE ≤ +1.0 D;
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Astigmatism of either eye less than -5.0 D;
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Anisometropia ≤ -1.5 D;
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There was no active ocular inflammatory diseases; no obvious corneal cloud or macula, anormal corneal topography, and no tendency of keratoconus.
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Intraocular pressure of either eye is of 10 to 21 mmHg;
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On the basis of full understanding, children and their guardians sign the informed consent;
Adults Inclusion Criteria
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adults aged 18-35
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Removing flexible lenses for at least 1 week, flexible astigmatism and hard lenses for at least 3 weeks, orthokeratology lenses for at least 3 months;
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Best corrected visual acuity of either eye were all ≥ 1.0;
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The range of myopia in either eye was -15 D ≤ SE ≤ +1.0 D;
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Astigmatism of either eye less than -5.0 D;
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Anisometropia ≤ -1.5 D;
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There was no active ocular inflammatory diseases; no obvious corneal cloud or macula, anormal corneal topography, and no tendency of keratoconus.
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Intraocular pressure of either eye is of 10 to 21 mmHg;
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On the basis of full understanding, adults sign the informed consent;
Exclusion Criteria:
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Amblyopia: best corrected visual acuity (BCVA) of either eye less than 1.0 for adults and children over 6 years old;
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Active ocular inflammatory diseases, such as uveitis and other inflammatory diseases;
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Secondary myopia, genetic disease or connective tissue- related myopia;
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Moderate or severe ptosis;
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Congenital cataract, glaucoma;
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Other fundus diseases other than myopic related fundus lesions;
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Intraocular or refractive surgery history;
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The refractive medium is turbid, and it is impossible to take a clear fundus image; (9)Unable to cooperate with fundus image shooting and other examination;
(10)Do not receive cycloplegia or have contraindications; (11)Poor overall condition, unable to follow up for a long time; (12)The subject refuses to participate in the research; (13)Other cases in which the researcher judges that it is not suitable for participation in the study.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Beijing Tongren Hospital, Capital Medical University | Beijing | Beijing | China | 100073 |
Sponsors and Collaborators
- Beijing Tongren Hospital
- Tsinghua University
Investigators
- Principal Investigator: Shi-Ming Li, Beijing Tongren Hospital
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 010133